Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K093360 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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OPTETRAK LOGIC Polyethylene Tibial Inserts, labeled as the following: a. OPTETRAK Logic PS Tibi... | 2 | 10/04/2021 | Exactech, Inc. |
OPTETRAK LOGIC TIBIAL INSERT POSTERIOR STABILIZED***Match Component Colors 6 YELLOW, 11mm, Use with ... | 2 | 09/04/2012 | Exactech, Inc. |
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